CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 156 enrolled
Drug / intervention
Meningococcal conjugate vaccine GSK134612biological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01777308
NCT01777308Phase 3Completed

The Vaccine Response and Long-term Antibody Persistence of GSK Biologicals' MenACWY-TT Vaccine (GSK134612) Administered as One Dose at 6 Years Post-MenC Primary Vaccination in Healthy Subjects Aged 12-18 Months at Primary Vaccination

GlaxoSmithKline·interventional·Posted Jan 28, 2013·Updated Jan 25, 2019

In Brief

A Phase 3 clinical trial evaluating Meningococcal conjugate vaccine GSK134612 for Infections, Meningococcal. Completed, enrolled 156 participants across 8 sites.

Detailed Summary

The purpose of this study is to evaluate the immunogenicity, reactogenicity and safety of a booster dose of GSK Biologicals' MenACWY-TT vaccine administered at 6 years post-primary vaccination with either GSK Biologicals' Hib-MenC-TT vaccine (Menitorix™) or Hiberix™ and Meningitec™, in healthy subjects aged 12-18 months at primary vaccination and to evaluate the long-term antibody persistence at 2 years after MenACWY-TT booster vaccination. This is an extension study of the Hib-MenC-TT-016 study (NCT number: NCT00326118).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJan 28, 2013
Enrollment StartMay 3, 2013
Primary CompletionJul 3, 2014
Study CompletionApr 20, 2016
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 13.4 years ago

Interventions

Meningococcal conjugate vaccine GSK134612biological

Single dose to be administrated intramuscularly in the deltoid of the non-dominant arm